By John M. S. Bartlett
Over 100 well-respected scientists comprehensively overview each element of the biology underlying ovarian melanoma and current a remarkably particular number of easy-to-follow tools for illuminating easy mechanisms underlying all kinds of melanoma. the following modern investigators will locate the broadest possible array of molecular biology ideas particularly designed to figure out not just tumor genetics, expression, and protein functionality, but additionally to clarify the genetic mechanisms wherein gene and immunotherapies can be perfected. flexible and accomplished, Ovarian melanoma tools and Protocols constitutes a veritable treasury of well-proven professional tools that may aid simple scientists and medical researchers alike grasp the robust applied sciences required for powerful melanoma study at the present time.
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Extra info for Ovarian Cancer: Methods and Protocols (Methods in Molecular Medicine)
1981) Familial excess of cancer of the ovary and other anatomic sites. JAMA 245, 261–264. 15. Hall, J. , Lee, M. , Morrow, J. , Anderson, L. , and King, M. C. (1990) Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250, 1684–1689. 16. Narod, S. , Lynch, H. , and Lenoir, G. M. (1991) Familial breast-ovarian cancer locus on chromosome 17q12-q23. Lancet 338, 82,83. 17. , Easton, D. , et al. (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families.
Breast Cancer Linkage Consortium. Am. J. Hum. Genet. 56, 265–271. 52. , McGovern, P. , Chiu, H. , Couch, F. , Weber, B. , et al. (1995) Mutation analysis of the BRCA1 gene in ovarian cancers. Cancer Res. 55, 2998–3002. 53. Stratton, J. , Gayther, S. , et al. (1997) Contribution of BRCA1 mutations to ovarian cancer. N. Eng. J. Med. 336, 1125–1130. 54. DudokdeWit, A. , Frets, P. , Meijers-Heijboer, E. , Klijn, J. , et al. (1997) BRCA1 in the family: a case description of the psychological implications.
Med. 339, 424–428. Molecular Pathogenesis of Ovarian Cancer 25 3 The Molecular Pathogenesis of Ovarian Cancer S. E. Hilary Russell 1. The Genetic Basis of Cancer In recent years, there has been considerable progress in understanding the molecular events that give rise to clonal tumor development. This is best described by the steps in the development of colorectal tumors in which the activation of cellular protooncogenes and inactivation of several tumor suppressor genes has been elucidated (1).